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Preclinical Reporting Module

Total Preclinical R&D Management Solution. Generate Reports Simply and Easily.

Book a Demo

Book a demo with us now to experience a tailored solution that specifically addresses your current business needs.

Reduce Compliance Risk

Implement an all-in-one digital cloud platform to be always ready to meet compliance needs.

Increase Efficiency​

Replace standalone applications and paper trails with fully customized digital solutions.

Reduce Cost by 30%

Compliance Embedded, Quality Engrained, Data Integrity Assured

Key Features of the Pristima XD Preclinical Reporting

You can save significant time with powerful reports that are easy to generate anytime you want visibility into your study. Key features of the Pristima XD Core Preclinical Reporting module:

Define Format and Content of Output Data Tables Produced in HTML, PDF, MS Office & CSV Format Full GLP and OECD Compliance

Filters to Produce Summarizations by Study, Animal, Date, Subgroup, and Dose Group Upon Demand

Tight Integration – All Data Stays under Pristima XD Control. Robust Embedded Statistical Analysis Capabilities Eliminate the Need for Third-Party Applications

Reports may be displayed on a screen, sent via email, or printed

Visualization of data using graphs.

Design, generate, distribute and schedule reports.

Pristima XD Software Modules

From subject acquisition through study submission, Pristima XD helps you manage the entire preclinical lifecycle.

Click a module to learn more about Pristima XD core features and benefits: